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We describe the behavior in captivity of the dusky shrew-opossum Caenolestes fuliginosus from 17 specimens captured at Finca La Martinica (Colombia), which were kept alive in plastic terraria for different periods of time (between 1 and 12 consecutive days). We found that C. fuliginosus can climb and jump well and uses its nonprehensile tail as a support when climbing. Feeding observations showed a preference towards an animalivorous diet, which included moths/butterflies (Insecta, Lepidoptera), stick-insects (Insecta, Phasmatoidea), flatworms (Platyhelminthes, Turbellaria), earthworms (Annelida, Oligochaeta), frogs (Amphibia, e.g., Pristimantis sp.), and dead rodents (Rodentia, Sigmodontinae, e.g., Microryzomys sp., Thomasomys sp.). Individuals were active throughout the day and night, with no indication of daily torpor. Our observations showed C. fuliginosus is not aggressive towards congeners and often aggregates during rest, especially when several individuals are placed together. Unlike other New World marsupials, C. fuliginosus showed nonagonistic group feeding behavior when consuming carcasses. Stereotyped behavior patterns (e.g., grooming) were not frequently observed. Our work provides comparative information for further studies on caenolestids and other New World marsupials. En este trabajo describimos el comportamiento en cautiverio del ratón Runcho, Caenolestes fuliginosus, a partir de la observación directa de 17 individuos capturados en Finca La Martinica (Colombia), que fueron mantenidos en terrarios plásticos por diferentes períodos de tiempo (entre 1 y 12 días consecutivos). Observamos que C. fuliginosus puede trepar y saltar bien, usando su cola no prensil como soporte al trepar. Los individuos mostraron preferencias alimenticias hacia una dieta animalívora que incluyó: polillas/mariposas (Insecta, Lepidoptera), insectos palo (Insecta, Phasmatoidea), gusanos planos de vida libre (Platyhelminthes, Turbellaria), lombrices (Annelida, Oligochaeta), ranas/sapos (Amphibia, e.g., Pristimantis sp.) y roedores muertos (Rodentia, Sigmodontinae, e.g., Microryzomys sp., Thomasomys sp.). Observamos actividad durante todo el día y la noche, sin preferencias, y no observamos torpor en ningún individuo. Los individuos no mostraron comportamiento agresivo hacia sus congéneres y, con frecuencia, se juntaron para descansar unos sobre otros. A diferencia de otros marsupiales del nuevo mundo, C. fuliginosus no mostró comportamiento agonístico cuando se alimenta de cadáveres. Patrones estereotipados de comportamiento (e.g., limpieza) no fueron frecuentemente observados. Nuestro trabajo aporta información comparativa para futuros estudios sobre el comportamiento de otros cenoléstidos y marsupiales del nuevo mundo.

We evaluate the occurrence of S. bakeri in Colombia, a recently described species. We report seven new records and include data on skull measurements of these individuals and information on the new localities. A discriminant analysis suggests that condyloincisive length and dentary length are the most important measurements to separate S. bakeri and S. luisi from S. lilium. However, to distinguish S. bakeri from S. luisi, we used discrete characters proposed in the original descriptions of these two taxa. Sturnira bakeri should no longer be considered a regionally endemic species from Ecuador and Peru.

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Background: Caenolestids are a group of poorly known South American marsupials with a restricted distribution in Páramo and Subpáramo environments of the Andes from Colombia and western Venezuela to Bolivia (represented by the genera Caenolestes and Lestoros), and Valdivian rainforest in southern Chile (including a separate population in Chiloé Island) and Argentina, where a single species lives: the Long-nosed shrew opossum (Rhyncholestes raphanurus). The objectives of this work were to analyze the intraspecific variability of R. raphanurus, which includes an anatomical description of the skull and dentition, describe its geographic variation, test for sexual dimorphism, and assess potential differences between continental and Island populations. Methods: Linear Mossimann-transformed variables were used to assess sexual differences within a large population (La Picada), compare sexes within other continental populations, and in a separate analysis, compare continental from Island samples. A full model Principal Components Analysis was performed to assess differences between males and females of the continental and Island populations. A thorough description of the skull and teeth of the species and comparisons with other living Caenolestidae is presented. Results: Rhyncholestes raphanurus presents little geographic variation, even between Island and continental populations. Similarly, we found no significant difference between sexes of this species in cranial and dental measurements. We provide a detailed description of cranial morphology and its variation, and also, the first description of the occipital bones, which haven't been previously described for any Paucituberculata. Conclusions: Comparative studies of continental and Chiloé Island specimens support the treatment of R. raphanurus as a single valid species, especially since morphologic and morphometric differences fall within the extremes of continental populations. The morphology of R. raphanurus clearly separates this genus from other extant Caenolestidae, and in a much greater degree than the differences found between Lestoros and Caenolestes.

Marmosini species were taxonomically revised recently, however, little is known about their distribution and conservation. The aim of this research was to delimit the distribution of all species of Marmosini that inhabit Colombia, and analyze their conservation using potential distributions, protected areas, and human pressure data of the country. We used the widely known ecological niche modeling algorithm maxent to model the distribution of each species using two approaches to estimate the modeling area: a buffer-derived and an ecoregion-derived. After selecting a final model, we used data on protected areas and human pressure specific to Colombia, and analyze their conservation and pressure scenarios. Finally, we generated a species richness map for Marmosini in Colombia. We found that most species of Marmosini from Colombia co-occur at mid-elevations of the Andes with an upper elevation limit of maximum richness at ~ 2000 m. Marmosini species’ distribution covers 91% of the country's continental area, and the maximum area protected for any species of this group is between 29–5.4% of their modeled distribution. Most of the protected areas under strict and national conservation types presented small areas of high human pressure, while other categories (conservation units under managed resources and other conservation types) presented large areas of high human pressure. These species are poorly protected by the Natural Protected Areas of Colombia. Future reserves that cover Andean regions below 2000 m could help optimize their conservation.

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